The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
870923121 8709231 21 F 20111122 20160920 20120806 20160922 EXP CA-ROCHE-785471 ROCHE 43.16 YR F Y 52.21000 KG 20160922 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
870923121 8709231 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) ON 29/OCT2015, SHE RECEIVED LAST DOSE OF RITUXIMAB. N3493B011,B622282,B62332,H06453,H06 103705 1000 MG SOLUTION FOR INFUSION
870923121 8709231 2 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) N3493B011,B622282,B62332,H06453,H06 103705 SOLUTION FOR INFUSION
870923121 8709231 3 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) N3493B011,B622282,B62332,H06453,H06 103705 SOLUTION FOR INFUSION
870923121 8709231 4 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) N3493B011,B622282,B62332,H06453,H06 103705 SOLUTION FOR INFUSION
870923121 8709231 5 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral D 0 25 MG 1X
870923121 8709231 6 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral D 0 50 MG
870923121 8709231 7 C CORTISONE CORTISONEHYDROCORTISONE 1 0
870923121 8709231 8 C TYLENOL ACETAMINOPHEN 1 0
870923121 8709231 9 C BIAXIN CLARITHROMYCIN 1 Oral 0 500 MG BID
870923121 8709231 10 C FLOVENT FLUTICASONE PROPIONATE 1 Unknown 0 125 UG
870923121 8709231 11 C NOVO-SALMOL 2 Unknown 2 PUFS 4 TIMES A DAY PRN 0 100 UG INHALATION VAPOUR
870923121 8709231 12 C PMS-HYDROMORPHONE HYDROMORPHONE HYDROCHLORIDE 1 Oral PRN 0 1 DF Q4H
870923121 8709231 13 C RATIO-SALBUTAMOL 2 Unknown 4-6 HOURS PRN 0 10 ML
870923121 8709231 14 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 0 INHALATION VAPOUR BID
870923121 8709231 15 C PREDNISONE. PREDNISONE 1 Unknown 0 2.5 MG QD
870923121 8709231 16 C CODEINE HYDROCHLORIDE CODEINE HYDROCHLORIDE 1 0
870923121 8709231 17 C DIPHENHYDRAMIN-HCL 2 Oral 0 50 MG
870923121 8709231 18 C DIPHENHYDRAMIN-HCL 2 Oral 0 50 MG
870923121 8709231 19 C DIPHENHYDRAMIN-HCL 2 Intravenous (not otherwise specified) 0 50 MG
870923121 8709231 20 C ACETAMINOFEN ACETAMINOPHEN 1 Oral 0 1000 MG
870923121 8709231 21 C ACETAMINOFEN ACETAMINOPHEN 1 Oral 0 650 MG
870923121 8709231 22 C ACETAMINOFEN ACETAMINOPHEN 1 Unknown 0 1000 MG
870923121 8709231 23 C ACETAMINOFEN ACETAMINOPHEN 1 Unknown 0 1000 MG
870923121 8709231 24 C ACETAMINOFEN ACETAMINOPHEN 1 Unknown 0 650 MG
870923121 8709231 25 C METHYLPREDNISOLON METHYLPREDNISOLONE 1 Unknown 0 100 MG
870923121 8709231 26 C METHYLPREDNISOLON METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 0 100 MG
870923121 8709231 27 C METHOTREXATE. METHOTREXATE 1 Unknown 0 10 MG /wk
870923121 8709231 28 C EURO-FOLIC 2 Unknown 0 5 MG BID
870923121 8709231 29 C RATIO-CODEINE 2 0
870923121 8709231 30 C FOLIC ACID. FOLIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
870923121 8709231 1 Rheumatoid arthritis
870923121 8709231 5 Throat irritation
870923121 8709231 6 Ear pruritus
870923121 8709231 17 Premedication
870923121 8709231 20 Premedication
870923121 8709231 25 Premedication

Outcome of event

Event ID CASEID OUTC COD
870923121 8709231 OT
870923121 8709231 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
870923121 8709231 Arthralgia
870923121 8709231 Arthritis
870923121 8709231 Asthma
870923121 8709231 Bacterial infection
870923121 8709231 Breath sounds abnormal
870923121 8709231 Choking
870923121 8709231 Dry throat
870923121 8709231 Dysphonia
870923121 8709231 Dyspnoea
870923121 8709231 Ear pruritus
870923121 8709231 Emphysema
870923121 8709231 Hypotension
870923121 8709231 Infusion related reaction
870923121 8709231 Leukoplakia
870923121 8709231 Lung neoplasm
870923121 8709231 Metastatic neoplasm
870923121 8709231 Nausea
870923121 8709231 Odynophagia
870923121 8709231 Oropharyngeal discomfort
870923121 8709231 Paraesthesia ear
870923121 8709231 Pharyngeal paraesthesia
870923121 8709231 Pneumonia
870923121 8709231 Pyrexia
870923121 8709231 Rheumatoid arthritis
870923121 8709231 Skin ulcer
870923121 8709231 Somnolence
870923121 8709231 Throat irritation
870923121 8709231 Vomiting
870923121 8709231 Weight decreased
870923121 8709231 Wound

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
870923121 8709231 5 20130128 20130128 0
870923121 8709231 17 20120725 20120725 0
870923121 8709231 18 20101124 0
870923121 8709231 19 20140310 0
870923121 8709231 20 20120725 20120725 0
870923121 8709231 21 20101124 0
870923121 8709231 22 20111122 0
870923121 8709231 23 20120712 0
870923121 8709231 24 20130129 0
870923121 8709231 25 20120725 20120725 0
870923121 8709231 26 20101124 0